Canonical Allele Identifier: CA339117840

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26139263T>A (hg19) ; chr1:g.25812772T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812772T>A , CM000663.2:g.25812772T>A	GRCh38
NC_000001.10:g.26139263T>A , CM000663.1:g.26139263T>A	GRCh37
NC_000001.9:g.26011850T>A	NCBI36
NG_009930.1:g.17597T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1196T>A	ENSP00000346109.5:p.Leu399Gln
ENST00000494537.2:c.1265T>A	ENSP00000508308.1:p.Leu422Gln
ENST00000361547.7:c.1367T>A MANE Select	ENSP00000355141.2:p.Leu456Gln
ENST00000354177.8:c.1265T>A	ENSP00000346109.4:p.Leu422Gln
ENST00000361547.6:c.1367T>A	ENSP00000355141.2:p.Leu456Gln
ENST00000374315.1:c.1265T>A	ENSP00000363434.1:p.Leu422Gln
ENST00000494537.1:n.45T>A
ENST00000559265.1:n.255+893T>A
ENST00000630065.2:c.-206T>A	ENSP00000487549.1:n.-206T>A
NM_020451.2:c.1367T>A	NP_065184.2:p.Leu456Gln
NM_206926.1:c.1265T>A	NP_996809.1:p.Leu422Gln
NM_020451.3:c.1367T>A MANE Select	NP_065184.2:p.Leu456Gln
NM_206926.2:c.1265T>A	NP_996809.1:p.Leu422Gln